Skip to main content
. 2002 Nov;40(11):4100–4104. doi: 10.1128/JCM.40.11.4100-4104.2002

TABLE 2.

Possible cases of laboratory cross-contamination detailing symptoms, therapy, and final diagnosis

Case Reason investigateda Anti-TB drugs Assessment conclusion
M CXR—upper zone shadowing, cavitation; clinically consistent Full course Presumed case of TB; no obvious epidemiological link to clustered cases possible laboratory contamination between two known cases
N CXR—upper zone shadowing and effusion; pleuritic chest pain Full course Treated as case of TB; symptoms and signs persisted posttreatment
O Fine-needle aspirate of persisting lymphadenopathy Unknown Unknown—case notes lost
P CXR—upper zone shadowing; clinically consistent Full course Presumed case of TB; no obvious epidemiological link to clustered cases: possible laboratory contamination between two known cases
Q CXR—effusion, pneumothorax; breathless, cachexia, persistent cough Unknown Known congestive cardiac failure and carcinoma of bronchus; diagnosis of TB uncertain; already transferred abroad for terminal care before culture result
R Unknown Unknown Case notes unobtainable
S HIV positive, low CD4 counts, febrile, cough Full course Multiple other samples isolated MAIC; probably not TB but possibility of dual infection, hence not denotified
T CXR—pleural effusion; immunocompromised post-renal transplant; past history of TB Full course Current diagnosis uncertain; fully treated in view of past history and immunocompromise
a

CXR, chest X ray; HIV, human immunodeficiency virus; MAIC, Mycobacterium avium-M. intracellulare complex; TB, tuberculosis.